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The Wheelchair When my dad was eighteen years old he went into the military, and was stationed overseas in Europe. One night, after having a few drinks with his friends and his commanding officer, he had to drive his commanding officer back to the base because he was not in a fit state to drive. It was late at night, very dark, and my dad didn’t really know where he was going. This resulted in my dad driving, and his commanding officer giving him directions. My dad was not 100% confident in his directions, but it was his commanding officer and you do what they say to do, when they say to do it. The man gave him a wrong direction, and it ended with them both toppling over a cliff and flipping the vehicle multiple times. Initially my Dad only …show more content…
Although I wasn’t even alive when he sustained his injury, his disability had a major impact my life. When I was born my dad had been in his wheelchair for about four years, and he had trouble taking care of himself let alone a newborn. My mom worked a full time job, and went to school, while my dad stayed home and was on disability. That left my dad, who could barely take care of himself, as my primary care giver. It was just me and him at the house for about ten hours a day. This sounds a little more scary than it actually was. My mom and dad knew this was going to be their way of life, and thanks to savings my Mom was able to stay home for the first six months of my life. During this time they remodelled and set the whole house up, as best they could, so that my dad could take care of me; change my diapers, make me food etc. Though my dad made me food, and changed my diapers, it was physically difficult for him to get off of the couch. This meant, as I got a little bigger, I had I had to get the food and diapers and bring them to the couch where he was so that he could cook my food in the microwave or so he could change my diaper. The fact that I had to retrieve my own basic necessities, caused me not only to walk before I was one, it also caused me to learn a sense of responsibility before I even knew what it
The Best Four Wheelchair Vans We Have Seen In 2013 It is hard to live with a disability, because everyday things become a challenge. A U.S. Census Bureau report from 2008 states that 3.3 million non-institutionalized Americans over age 15 use wheelchairs. The reason why there are so many people with disabilities is that the U.S. spent decades at war. This is why the mobility industry is rethinking the products it provides to support a growing demographic. Vantage Mobility International (VMI) and Braun Ability are two leading industry players that spent decades converting wheelchair vans from companies such as Chrysler, Toyota, and Honda into wheelchair-accessible modes of transportation.
In the book, The Short Bus, Jonathan Mooney’s thesis is that there is more to people than their disabilities, it is not restricting nor is it shameful but infact it is beautiful in its own way. With a plan to travel the United States, Mooney decides to travel in a Short bus with intentions of collecting experiences from people who have overcome--or not overcome--being labeled disabled or abnormal. In this Mooney reinvents this concept that normal people suck; that a simple small message of “you’re not normal” could have a destructive and deteriorating effect. With an idea of what disabilities are, Mooney’s trip gives light to disabilities even he was not prepared to face, that he feared.
The Moving Beyond Pity & Inspiration: Disability as a social Justice Issue by Eli Clare took place on April 16, 2014. Thinking about disability before this lecture I feel like I had a general idea of the things Eli spoke about. I attended a school were more than half of the students had a disability. The terms and stereotypes he mentioned I ha heard since sixth grade.
What is there left to do when helping someone disabled is completely out of our reach because it is impossible to look after them every second of the day? In the story Of Mice and Men, one issue John Steinbeck mentions throughout the book is the relationship between George and Lennie vs. Lennie’s disability. Lennie is a big strong man, capable of seriously hurting anyone, with the mentality of a child which sets George back on his own dreams for the reason that Lennie cannot care for himself. They have to travel together for this reason and as tough as it is already watching over Lennie, they are running away from an incident that happened in Weed, their previous job. Lennie‘s disability is the main conflict and because he is not fully capable of understanding how to control himself fully, he is not to be fully blamed for his mistakes; which in fact, all lead to the exposition, climax, and resolution of the story. Curley, the boss’s son, becomes threatened by Lennie’s large appearance and Curley’s wife flirtatious personality is a problem when Lennie could easily fall into her traps and all this leads to Lennie’s death.
At 10, I never knew whether my father would be sober, reasonable, even pleasant - or drunk, argumentative and abusive. On one February day with four inches of snow on the ground and a freezing rain falling, I was walking home from my cousin's house in the early evening and saw my father lying on the soggy, snow-covered sidewalk. I didn't know what my father would do if I roused him, and I was afraid to find out. Perhaps, subconsciously, I hoped my father wouldn't waken at all. I continued on, did nothing, said nothing. This I will remember with guilt for the rest of my life.
Before I was born, my grandfather was involved in numerous surgeries on his left knee to fix torn ligaments as a result of his line of work. As time went on, the physical effort took a toll on his good knee, prompting additional surgeries. At the time, doctors suggested a bone or joint fusion surgery to help with the type of injury he sustained. It was a permanent procedure ultimately resulting in the inability to bend at the joint and making his left leg two inches shorter than his right. Everyday tasks that I had taken for granted, such as driving a car, using the restroom, and even standing for long periods of time became impediments to daily living. Having heard about this traumatic and chronic experience, it remained in the back of my mind for some time. It was not until I was 13 years old when I had my first encounter with an occupational therapist during an appointment that I
All throughout Elementary school teachers and parents would say, “Sticks and stones may break your bones, but words will never hurt you”, but in a way they were wrong. My father married my step-mother who had two children around my age. The oldest was a very normal kid, but the second was autistic. Despite his autism, he was a very sweet kid and when it came to the subject of animals he was a genius, however this made no difference to his peers. He would be referred to as “retard” or other hurtful names behind his back. His brother, himself, and myself all went to the same school and his brother and I would have to deal with these immature students. They would pick on him constantly, but the saddest part is he could never tell that they were picking on him; in his mind he thought that was how everyone played. I would have to talk to these students, but they never understood the problem, “he can’t tell” or “he’s having fun” they would say. In no way does that make it right. Just because someone can’t tell that you are picking on them or doesn’t hear you say the hurtful comments, shouldn’t allow you to disrespect them.
Physical therapy is always full of surprises, from new advancements in technology to new and improved therapeutic techniques. Although there are fun games and new technology that physical therapists can do with patients, the main struggle for physical therapists is to motivate their patients to complete their therapy exercises both in the clinic and in the outside world. This problem is very frustrating because the doctors who work at the clinic constantly push patients to complete their therapy so that they can heal; however, when patients are stubborn and reluctant to their treatment, yet constantly complain of pain, doctors must spend more time convincing them to do the therapy rather than completing the therapy itself.
Deaf Culture is often misunderstood because the hearing world thinks of deafness as a handicap. The Deaf are not given enough credit for their disabilities even though they are unable to hear. Being misunderstood is the biggest reason why they are not accepted in the world of hearing. The learning process for them may be slower and more difficult to learn, but they are still very bright individuals. The problem at hand is the controversy of trying to “fix” the Deaf when they may or may not want to be “fixed”. The hearing world should give Deaf people a chance to show their true talents and abilities of intelligence before rushing to assumptions, such as hearing aids will fix all Deaf people, because Deaf are dumb, have social problems, and
It can be difficult and frustrating not to be able to do certain things at first, but it is not any different for someone who is not in a wheelchair. People often doubt their abilities and therefore have low expectations of them. What people fail to see is how mentally capable and hardworking these individuals truly are. Axel recalls, “Growing up in a wheelchair made the people around me assume that I wouldn’t be able to do anything for myself and that only motivated me more to be independent and prove not only to myself, but to others that being in a wheelchair doesn’t mean I can’t do what a normal person does, like driving, playing sports, or the basics of going to the restroom on my own.” People like Axel know that being physically disabled does not mean that they can not do what any other normal person does.
When I was seventeen I nervously traveled about 350 miles from my sleepy little home town of Freedom, Wyoming to the relatively enormous city of Boise, Idaho to go to the Military Entrance Processing Station. This wasn 't the first time I had been this far from home by myself, but it was the first time I was making adult decisions without my parents involvement. When it came time for me to choose my job in the army the counselors presented me with a long list that I qualified for. I got tired of scrolling and reading so I chose the first job that I actually understood. I returned home and excitedly told my parents that I would be an infantry soldier. My dad 's response to this might be considered a little less than heart warming “You dumb ass. Why didn 't you choose
This essay will explore the medical model of disability as well as the social model of disability by providing an in depth analysis of the views and explanations that outline each perspective. It will examine and establish the connection of the two models in relation to Deaf people. Furthermore it will illustrate how Deaf people are defined according to each outlook, as well as the issues and concerns that arise from these perceptions. This essay will consider the medical model and the social model to compare the ideas and objectives of the given articles; Caught in the Deaf Trap by Karen Van Rooyen, A Brave New World of Sound by Thandi Skade, Fake Interpreters: A Violation of Human Rights and lastly Professor Graham Turner’s; 10 lessons from the tale of the ‘fake’ interpreter.
Self-care often goes over looked. However, it could be one of the most important things a healthcare professional can do for themselves and the patients. Working in healthcare often consists of long hours and lots of brain power. Your mind is always on and you are always on high alert. That can be taxing on our minds, bodies, and souls. This is where self-care comes into play. Decompression can look like many things. I some play golf. Others take bi-monthly trips to the massage parlor. Some people seek solace in prayer and meditation. It is important to understand that self-care is not limited to people who hold huge responsibilities. These are techniques everyone should utilize as much as possible.
As a grandson and nephew of a disabled grandmother and aunt, the struggle of disability is commonly experience in our family an...
Disability: Any person who has a mental or physical deterioration that initially limits one or more major everyday life activities. Millions of people all over the world, are faced with discrimination, the con of being unprotected by the law, and are not able to participate in the human rights everyone is meant to have. For hundreds of years, humans with disabilities are constantly referred to as different, retarded, or weird. They have been stripped of their basic human rights; born free and are equal in dignity and rights, have the right to life, shall not be a victim of torture or cruelty, right to own property, free in opinion and expression, freedom of taking part in government, right in general education, and right of employment opportunities. Once the 20th century